Metaxalone
Product Images NDC 68387-108

3 FDA label images from Keltman Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metaxalone (NDC 68387-108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Keltman Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (0aff6dda B9fd 4f01 85b2 Eb3097b760b0 01)

Chemical Structure (0aff6dda B9fd 4f01 85b2 Eb3097b760b0 01)
Chemical structure diagram of the active ingredient Metaxalone, showing its molecular arrangement including methyl groups, an ether linkage, and a morpholinone ring.*
FDA Label Image

Figure 1 (0aff6dda B9fd 4f01 85b2 Eb3097b760b0 02)

Figure 1 (0aff6dda B9fd 4f01 85b2 Eb3097b760b0 02)
A line graph comparing Metaxalone concentration (ng/mL) in plasma over time (hours) between fasted and fed states. The graph shows higher concentrations and a later peak in the fed state (solid circles) compared to the fasted state (open circles), with error bars indicating variability at each time point.*
FDA Label Image

Metaxalone 800 mg Label (Metaxalone 800mg)

Metaxalone 800 mg Label (Metaxalone 800mg)
Metaxalone 800 mg tablet label from Keltman Pharmaceuticals Inc. The label indicates it is a generic version of Skelaxin 800 mg, with 30 tablets per package. It includes lot number 1044991, expiration date 4/2013, and instructions to store at controlled room temperature. The label also provides manufacturer and distributor information and a caution about federal law restricting drug transfer.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.